RPGRIP1-like
The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5).
Mouse Anti-RPGRIP1L Antibody (CBMOAB-56742FYA) (CAT#: CBMOAB-56742FYA)
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- Host species: Mouse
- Species Reactivity: Rhesus (Macaca mulatta), Chimpanzee (Pan troglodytes), Zebrafish (Danio rerio)
- Application: WB, ELISA
- Protein: Submitted name: RPGRIP1 like
- Size: 0.5mg, 1mg, 200µg
- Conjugate: Alexa Fluor 350, AP, APC, Biotin, Consult us more, Cy3, Cy5, Cy5.5, Cy7, FITC, HRP, NONE, PE, PerCP
- Alternative Names: RPGRIP1L
For Research Use Only | Not For Clinical Use.
